Insertion in the cysteine-rich domain (CRD) that results in a truncated protein being produced.
Insertion into the first exon that shifts the reading frame.
abnormal neuroanatomy | P-stage (with fz15)
male fertile (with fz23)
visible | adult stage (with fz30)
leg, with fz4C3.Act5C
leg, with fz6E3.Act5C
leg, with fz7A3.Act5C
leg, with fz8A4.Act5C
leg, with fz8F2.Act5C
leg, with fz11A2.Act5C
leg, with fz14B2.Act5C
leg, with fz17A1.Act5C
leg, with fz18B3.Act5C
leg, with fz19D3.Act5C
leg, with fz25A3.Act5C
leg, with fz25B2.Act5C
leg, with fz26C1.Act5C
leg, with fz26C2.Act5C
leg, with fz27C2.Act5C
leg, with fz30A3.Act5C
leg, with fz30E2.Act5C
leg, with fz37E2.Act5C
leg, with fz39B2.Act5C
leg, with fz39D1.Act5C
leg, with fz47B3.Act5C
leg, with fz50E1.Act5C
leg, with fz68G2.Act5C
leg, with fz70A2.1.Act5C
leg, with fz70A2.3.Act5C
leg, with fz70B4.Act5C
leg, with fz72A4.Act5C
leg, with fz73A2.Act5C
leg, with fz76B1.Act5C
leg, with fz79F3.Act5C
leg joint | ectopic, with fz4C3.Act5C
leg joint | ectopic, with fz6E3.Act5C
leg joint | ectopic, with fz7A3.Act5C
leg joint | ectopic, with fz8A4.Act5C
leg joint | ectopic, with fz8F2.Act5C
leg joint | ectopic, with fz11A2.Act5C
leg joint | ectopic, with fz14B2.Act5C
leg joint | ectopic, with fz17A1.Act5C
leg joint | ectopic, with fz18B3.Act5C
leg joint | ectopic, with fz19D3.Act5C
leg joint | ectopic, with fz25A3.Act5C
leg joint | ectopic, with fz25B2.Act5C
leg joint | ectopic, with fz26C1.Act5C
leg joint | ectopic, with fz26C2.Act5C
leg joint | ectopic, with fz27C2.Act5C
leg joint | ectopic, with fz30A3.Act5C
leg joint | ectopic, with fz30E2.Act5C
leg joint | ectopic, with fz37E2.Act5C
leg joint | ectopic, with fz39B2.Act5C
leg joint | ectopic, with fz39D1.Act5C
leg joint | ectopic, with fz47B3.Act5C
leg joint | ectopic, with fz50E1.Act5C
leg joint | ectopic, with fz68G2.Act5C
leg joint | ectopic, with fz70B4.Act5C
leg joint | ectopic, with fz72A4.Act5C
leg joint | ectopic, with fz73A2.Act5C
leg joint | ectopic, with fz76B1.Act5C
leg joint | ectopic, with fz79F3.Act5C
macrochaeta & adult thorax
trichome & pleural membrane, with Scer\GAL4hh-Gal4, fzUAS.cSa
Mutant adults have an average of 2.9 +/- 0.6 extra tarsal joints in the leg compared to wild type.
The orientation of trichomes is uniformly randomised only in the most central region of the notum in mutant animals.
Homozygous clones in the notum nonautonomously influence the polarity of neighbouring bristles and trichomes.
fz21 mutant wings display strong hair orientation defects, but very few if any multiple hairs.
Prehair initiation is delayed in mutant cells away from the clone edge in homozygous clones in the wing.
The hexagonal packing of intervein cells, which usually occurs between wing development stage P2B (when the first morphological signs of veins appear (FBrf0005070), and the middle of P2C (before hair formation (FBrf0005070)) is partially disrupted in fz21/fz21 flies.
Mutant clones in the wing result in domineering nonautonomy wing hair polarity phenotype.
Somatic clones in the wing disc do not exhibit significant delay in hair development.
Mutant clones in the wing show domineering non-autonomy: cells distal to the clone, as well as within the clone, show alteration of polarity of wing hairs.
Homozygous somatic clones in the wing cause domineering non-autonomy.
Dendritic development in fz21/Df(3L)fz-D21 mutants is indistinguishable from wild-type.
Non-autonomous phenotype in wing clones.
Moderate thoracic bristle phenotype; moderate wing-hair disorientation.
fz21/fz19 has abnormal planar polarity | adult stage phenotype, non-enhanceable by Ror[+]/Ror4
fz21/fz19 has abnormal planar polarity | adult stage phenotype, non-enhanceable by Ror4/Ror4
fz23/fz21 has abnormal planar polarity | adult stage phenotype, non-enhanceable by Ror[+]/Ror4
fz23/fz21 has abnormal planar polarity | adult stage phenotype, non-enhanceable by Ror4/Ror4
fz21 has abnormal planar polarity phenotype, non-enhanceable by pkpk-sple-13/pkpk-sple-13
fz21 has abnormal planar polarity phenotype, non-enhanceable by pksple.UAS/Scer\GAL4hh-Gal4
fz21/fz19 has abnormal planar polarity phenotype, suppressible by Egfr[+]/Egfrtop-18A
fz23/fz21 has abnormal planar polarity phenotype, suppressible by fz::fz21-1-2S.tub.W
fz23/fz21 has abnormal planar polarity phenotype, suppressible by fz::fz21-2-1.tub.W
fz23/fz21 has abnormal planar polarity phenotype, suppressible by fz::fz21-1-2.tub.W
fz21 has abnormal planar polarity | somatic clone | cell non-autonomous phenotype, suppressible by inIH56/inunspecified
fz21/fz19 has abnormal planar polarity | adult stage phenotype, non-suppressible by Ror[+]/Ror4
fz21/fz19 has abnormal planar polarity | adult stage phenotype, non-suppressible by Ror4/Ror4
fz23/fz21 has abnormal planar polarity | adult stage phenotype, non-suppressible by Ror[+]/Ror4
fz23/fz21 has abnormal planar polarity | adult stage phenotype, non-suppressible by Ror4/Ror4
fz21 has abnormal planar polarity | somatic clone phenotype, non-suppressible by Vangstbm-6
fz23/fz21 has abnormal planar polarity | somatic clone phenotype, non-suppressible by fz::fz22-1-1.tub.Tag:MYC
fz21 has abnormal planar polarity | somatic clone | cell non-autonomous phenotype, non-suppressible by dsh3/dsh3
fz21 has abnormal planar polarity | somatic clone | cell non-autonomous phenotype, non-suppressible by pkpk-sple-13/pkpk-sple-13
fz21 has abnormal planar polarity phenotype, non-suppressible by pkpk-sple-13/pkpk-sple-13
fz21 has abnormal planar polarity phenotype, non-suppressible by pksple.UAS/Scer\GAL4hh-Gal4
fz23/fz21 has abnormal planar polarity phenotype, non-suppressible by fz::fz21-2-2.tub.W
fz23/fz21 has abnormal planar polarity phenotype, non-suppressible by fz::fz22-1-1.tub.W
fz21 has abnormal planar polarity | somatic clone | cell autonomous phenotype, non-suppressible by inIH56/inunspecified
fz21 has abnormal planar polarity | somatic clone | cell non-autonomous phenotype, non-suppressible by inIH56
fz21/fz15 is an enhancer of abnormal planar polarity phenotype of Scer\GAL4Bx-MS1096, kermitUAS.cLa
fz21 is an enhancer of abnormal planar polarity | recessive phenotype of Rab2351
fz21/fz30 is a suppressor of abnormal planar polarity phenotype of Scer\GAL4ptc.PU, fyUAS.GFP, inUAS.Tag:HA
fz[+]/fz21 is a suppressor | partially of abnormal planar polarity phenotype of fwsev.Tag:HA
fz[+]/fz21 is a suppressor | partially of abnormal planar polarity phenotype of Egfrt1/Egfrf11
fz[+]/fz21 is a suppressor of abnormal planar polarity | dominant phenotype of Egfrf24
fz21 is a suppressor of abnormal planar polarity | somatic clone phenotype of Vangstbm-6
fz21/fz21 is a suppressor of abnormal planar polarity | somatic clone phenotype of Scer\GAL4αTub84B.PL, pwnunspecified, stanUAS.cUa
fz21/fz21 is a suppressor of abnormal planar polarity | somatic clone | cell non-autonomous phenotype of Scer\GAL4αTub84B.PL, pwnunspecified, stanUAS.cUa
fz37/fz21 is a suppressor of abnormal planar polarity phenotype of Scer\GAL4ptc-559.1, stanUAS.cUa
fz2C1, fz21/fz15 has abnormal neuroanatomy | P-stage phenotype
fz2C1, fz21 has visible | somatic clone phenotype
chas1, fz21 has abnormal planar polarity phenotype
fz21 has trichome & adult abdomen phenotype, non-enhanceable by pkpk-sple-13/pkpk-sple-13
fz21 has trichome & adult abdomen phenotype, non-enhanceable by pksple.UAS/Scer\GAL4hh-Gal4
fz21/fz19 has ommatidium phenotype, suppressible by Egfr[+]/Egfrtop-18A
fz23/fz21 has eye phenotype, suppressible by fz::fz21-1-2.tub.W
fz23/fz21 has eye phenotype, suppressible by fz::fz21-1-2S.tub.W
fz23/fz21 has eye phenotype, suppressible by fz::fz21-2-1.tub.W
fz23/fz21 has wing hair phenotype, suppressible by fz::fz21-1-2.tub.W
fz23/fz21 has wing hair phenotype, suppressible by fz::fz21-1-2S.tub.W
fz23/fz21 has wing hair phenotype, suppressible by fz::fz21-2-1.tub.W
fz21 has wing hair | somatic clone | cell non-autonomous phenotype, suppressible by inIH56/inunspecified
fz21 has wing hair | somatic clone phenotype, non-suppressible by Vangstbm-6
fz23/fz21 has wing hair | somatic clone phenotype, non-suppressible by fz::fz22-1-1.tub.Tag:MYC
fz21 has wing hair | somatic clone | cell non-autonomous | pupal stage phenotype, non-suppressible by dsh3/dsh3
fz21 has wing hair | somatic clone | cell non-autonomous | pupal stage phenotype, non-suppressible by pkpk-sple-13/pkpk-sple-13
fz21 has trichome & adult abdomen phenotype, non-suppressible by pkpk-sple-13/pkpk-sple-13
fz21 has trichome & adult abdomen phenotype, non-suppressible by pksple.UAS/Scer\GAL4hh-Gal4
fz23/fz21 has eye phenotype, non-suppressible by fz::fz21-2-2.tub.W
fz23/fz21 has eye phenotype, non-suppressible by fz::fz22-1-1.tub.W
fz23/fz21 has wing hair phenotype, non-suppressible by fz::fz21-2-2.tub.W
fz23/fz21 has wing hair phenotype, non-suppressible by fz::fz22-1-1.tub.W
fz21 has wing hair | somatic clone | cell autonomous phenotype, non-suppressible by inIH56/inunspecified
fz21 has wing hair | somatic clone | cell non-autonomous phenotype, non-suppressible by inIH56
fz21/fz15 is an enhancer of wing hair phenotype of Scer\GAL4Bx-MS1096, kermitUAS.cLa
fz21/fz15 is an enhancer of wing hair | increased number phenotype of Scer\GAL4Bx-MS1096, kermitUAS.cLa
fz[+]/fz21 is a non-enhancer of wing hair phenotype of Scer\GAL4en-e16E, kermitGS2053
fz[+]/fz21 is a suppressor | partially of ommatidium phenotype of fwsev.Tag:HA
fz[+]/fz21 is a suppressor | partially of ommatidium phenotype of Egfrt1/Egfrf11
fz[+]/fz21 is a suppressor of ommatidium phenotype of Egfrf24
fz21 is a suppressor of wing hair | somatic clone phenotype of Vangstbm-6
fz21/fz21 is a suppressor of trichome & adult abdomen | somatic clone | cell non-autonomous phenotype of Vangstbm-6
fz[+]/fz21 is a non-suppressor of wing hair phenotype of Scer\GAL4en-e16E, kermitGS2053
fz2C1, fz21 has wing margin bristle | somatic clone phenotype
fz2C1, fz21 has wing margin | somatic clone phenotype
fz2C2, fz21 has wing margin bristle | somatic clone phenotype
fz2C2, fz21 has wing margin | somatic clone phenotype
Df(3L)fz2/+, fz21 has embryonic/first instar larval cuticle phenotype
Df(3L)fz2, fz21 has larval RP2 motor neuron phenotype
Df(3L)fz2, fz21 has cardioblast phenotype
Df(3L)fz2, fz21 has embryonic midgut constriction phenotype
The characteristic swirl of wing hairs seen on the ventral surface of the wing in animals co-expressing fyScer\UAS.T:Avic\GFP and inScer\UAS.T:Ivir\HA1 under the control of two copies of Scer\GAL4ptc.PU is not seen in a fz21/fz30 background.
fz21/+ partially suppresses the planar cell polarity defects in the eye caused by expression of two copies of fwsev.T:Ivir\HA1.
fz15/fz21 enhances the wing defects caused by expressing kermitScer\UAS.cLa under the control of Scer\GAL4Bx-MS1096, with a significant increase in the number of wing cells with multiple hairs.
Vangstbm-6 clones in the pupal wing in a uniformly fz21 background show no difference in the time of prehair initiation between single and double mutant tissue.
fz21 clones in the pupal wing in a uniformly Vangstbm-6 background show prehairs initiating sooner in Vangstbm-6 mutant tissue than in Vangstbm-6 ; fz21 double mutant tissue.
The planar cell polarity defects seen in Egfrf11/Egfrt1 eyes are partially suppressed by fz21/+.
The symmetrical ommatidium phenotype seen in fz19/fz21 flies is suppressed by Egfrtop-18A/+.
The frequency of rotation defects in the ommatidia of Egfrf24/+ flies is reduced to 12% or 18% respectively if they are also carrying fz21/+.
As is seen with fz21 clones alone, fz21 Vangstbm-6 double mutant clones non-autonomously reorient the wing hairs of neighbouring wild type cells so that they point towards the clone.
Expression of fz::fz22-1-1.tub.T:Hsap\MYC fails to rescue the non-autonomous effects of fz23/fz21 mutant clones on the orientation of the wing hairs of neighbouring wild type cells.
Vangstbm-6/Vangstbm-6 fz15/fz21 clones in the pupal wing (32 hours after puparium formation) have negligible effects on the polarity of trichomes in neighbouring cells. Trichome polarity is also relatively unperturbed within the double mutant clones.
stanE59 fz21 double mutant clones in the pupal wing (23 hours after puparium formation) do not affect polarity of trichomes in surrounding wild-type tissue.
dsh3 fz21/fz21 clones in the pupal wing (32 hours after puparium formation) cause neighbouring cells to point their trichomes towards the clone, as occurs with fz21/fz21 single mutant clones in the pupal wing.
pkpk-sple-13 fz21/fz21 clones in the pupal wing (32 hours after puparium formation) cause neighbouring cells to point their trichomes towards the clone, as occurs with fz21/fz21 single mutant clones in the pupal wing.
No evidence of a domineering nonautonomy wing hair polarity phenotype is seen in fz21 clones in a frtzunspecified background.
fz2ΔCRD.αTub84B.T:wg,T:Ivir\HA1 suppresses loss of naked cuticle in fz21/fz21, Df(3L)fz2/+ embryos. The additional presence of fz3G10/fz3G10 has no effect on this phenotype or its suppression. Somatic clones of cells homozygous for fz21 and fz2C2 at the anterior wing margin block the formation of wing margin bristles and cause wing notching. These phenotypes are fully suppressed by fz1-1-1.αTub84B, fz2αTub84B.PC, fzΔCRD.αTub84B.T:wg,T:Ivir\HA1 or fz2ΔCRD.αTub84B.T:wg,T:Ivir\HA1.
The planar polarity phenotype in the abdomen of fz21/fz21 flies is largely unaffected when the whole animal is also pksple.Scer\UAS and Scer\GAL4hh-Gal4 or pkpk-sple-13/pkpk-sple-13.
The loss of polarity seen adjacent to Vangstbm-6 somatic clones in the adult abdomen is suppressed by fz21/fz21.
The zone of reversed polarity at the back and behind the anterior compartment of each abdominal segment of stanScer\UAS.cUa; Scer\GAL4ptc-559.1 adults is suppressed by fz37/fz21.
When a wing clone is doubly mutant for fz21 and inIH56, domineering nonautonomy of polarity defect of fz21 is unaffected. When a wing clone is doubly mutant for fz21 and inIH56 in a genetic background deficient for in, domineering nonautonomy of polarity defect of fz21 is suppressed, though polarity defect within the clone is not.
Double mutants with Df(3L)fz2 show variable segmentation defects ranging from a few extra denticles in the posterior part of some segments to complete replacement of naked cuticle with denticles. This phenotype is reminiscent of that for wg loss of function. The expression of armΔN.Scer\UAS driven by Scer\GAL4da.G32 completely overrides this phenotype, causing naked cuticle. Double mutants with Df(3L)fz2 show a complete loss of RP2 neurons in all hemisegments. In double mutants of fz21 or fz23 with Df(3L)fz2 cardiac precursors are missing. Double mutants of fz21 or fz23 with Df(3L)fz2 lack the normal number of midgut constrictions. Overexpression of wgScer\UAS.cLb by Scer\GAL4da.G32 has no effect on the cuticle phenotype of double mutants of fz21 or fz23 with Df(3L)fz2.
fz21 is rescued by fzAct5C.PS
fz23/fz21 is rescued by fztub.Tag:MYC
fz23/fz21 is rescued by fz565Stop.tub.Tag:MYC
fz23/fz21 is rescued by fz1-1-1.tub.W
fz21 is rescued by Scer\GAL4da.G32/fzUAS.cAa
fz23/fz21 is not rescued by fzΔCRD.tub.Tag:MYC
fz23/fz21 is not rescued by fzΔSWRNF.tub.Tag:MYC
fz23/fz21 is not rescued by fzΔSKT.tub.Tag:MYC
fz23/fz21 is not rescued by fzM469R.tub.Tag:MYC
fzAct5C.PS rescue the ectopic leg joint phenotype seen in fz21 flies.
fzAct5C.PS fully rescues the wing margin phenotype of fz21 fz2C1 double homozygous clones.
Expression of fzΔCRD.tub.T:Hsap\MYC fails to rescue the non-autonomous effects of fz23/fz21 mutant clones on the orientation of the wing hairs of neighbouring wild type cells. 92.3% of clones have surrounding wild type cells pointing towards the clone.
Expression of fztub.T:Hsap\MYC rescues the wing hair phenotype seen in fz21/fz23 mutants.
Expression of fzΔSWRNF.tub.T:Hsap\MYC fails to rescue the wing hair phenotype seen in fz21/fz23 mutants.
Expression of fzΔSKT.tub.T:Hsap\MYC fails to rescue the wing hair phenotype seen in fz21/fz23 mutants.
Expression of fzM469R.tub.T:Hsap\MYC fails to rescue the wing hair phenotype seen in fz21/fz23 mutants.
Expression of fz565Stop.tub.T:Hsap\MYC rescues the wing hair phenotype seen in fz21/fz23 mutants.
Adler.